Department of Anesthesiology, Duke University Medical Center and Durham Veterans Affairs Medical Center, Durham, North Carolina, USA.
Anesthesiology. 2011 Feb;114(2):318-29. doi: 10.1097/ALN.0b013e3182065c36.
The management of elderly patients can be challenging for anesthesiologists for many reasons, including altered pharmacokinetics and dynamics. This study compared the efficacy, safety, and pharmacokinetics of sugammadex for moderate rocuronium-induced neuromuscular blockade reversal in adult (aged 18-64 yr) versus elderly adult (aged 65 yr or older) patients.
This phase 3a, multicenter, parallel-group, comparative, open-label study enrolled 162 patients aged 18 yr and older, American Society of Anesthesiologists class 1-3, scheduled for surgery with general anesthesia and requiring neuromuscular blockade. After anesthesia induction, patients received rocuronium, 0.6 mg/kg, before tracheal intubation, with maintenance doses of 0.15 mg/kg as required. At the end of surgery, patients received sugammadex, 2.0 mg/kg, at reappearance of the second twitch of the train-of-four (TOF) for reversal. The primary efficacy variable was time from sugammadex administration to recovery of the TOF ratio to 0.9 or greater. Pharmacokinetics and safety were also evaluated.
Overall, 150 patients were treated and had at least one postbaseline efficacy assessment; 48 were aged 18-64 yr (adult), 62 were aged 65-74 yr (elderly), and 40 were aged 75 yr or older (old-elderly). The geometric mean time (95% confidence interval) from sugammadex administration to recovery of the TOF ratio to 0.9 increased with age, from 2.3 (2.0-2.6) min (adults) to 2.9 (2.7-3.2) min (elderly/old-elderly groups combined). Recovery of the TOF ratio to 0.9 was estimated to be 0.7 min faster in adults compared with patients aged 65 yr or older (P = 0.022). Sugammadex was well tolerated by all patients.
Sugammadex facilitates rapid reversal from moderate rocuronium-induced neuromuscular blockade in adults of all ages.
由于药代动力学和药效动力学的改变等诸多原因,老年患者的管理对麻醉医师来说具有挑战性。本研究比较了舒更葡糖钠在成人(18-64 岁)与老年患者(65 岁或以上)中用于中度罗库溴铵诱导的神经肌肉阻滞逆转时的疗效、安全性和药代动力学。
这是一项 3a 期、多中心、平行分组、比较、开放标签研究,纳入了 162 名年龄 18 岁及以上、美国麻醉医师学会(ASA)分级 1-3 级、接受全身麻醉和需要神经肌肉阻滞的择期手术患者。麻醉诱导后,患者接受 0.6mg/kg 的罗库溴铵,以进行气管插管,根据需要给予 0.15mg/kg 的维持剂量。手术结束时,当出现四个成串刺激(TOF)的第二个颤搐时,患者给予舒更葡糖钠 2.0mg/kg 以逆转。主要疗效变量是从舒更葡糖钠给药到 TOF 比值恢复到 0.9 或更高的时间。还评估了药代动力学和安全性。
总体而言,150 名患者接受了治疗并至少进行了一次基线后疗效评估;48 名患者年龄在 18-64 岁(成人),62 名患者年龄在 65-74 岁(老年),40 名患者年龄在 75 岁或以上(老老年)。从舒更葡糖钠给药到 TOF 比值恢复到 0.9 的几何均数(95%置信区间)随年龄增加而增加,从 2.3(2.0-2.6)分钟(成人)增加至 2.9(2.7-3.2)分钟(老年/老老年组)。与 65 岁或以上的患者相比,成人恢复 TOF 比值至 0.9 的速度估计快 0.7 分钟(P=0.022)。所有患者均耐受良好。
舒更葡糖钠可促进各年龄段成人中中度罗库溴铵诱导的神经肌肉阻滞的快速逆转。